RU94041682A - Method of synthesis of taxane derivatives - Google Patents

Method of synthesis of taxane derivatives

Info

Publication number
RU94041682A
RU94041682A RU94041682/04A RU94041682A RU94041682A RU 94041682 A RU94041682 A RU 94041682A RU 94041682/04 A RU94041682/04 A RU 94041682/04A RU 94041682 A RU94041682 A RU 94041682A RU 94041682 A RU94041682 A RU 94041682A
Authority
RU
Russia
Prior art keywords
general formula
radical
synthesis
taxane derivatives
gmeans
Prior art date
Application number
RU94041682/04A
Other languages
Russian (ru)
Inventor
Депрэ Доминик
Fr]
Пюликани Жан-Пьер
Original Assignee
Рон-Пуленк Роре С.А. (FR)
Рон-Пуленк Роре С.А.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Рон-Пуленк Роре С.А. (FR), Рон-Пуленк Роре С.А. filed Critical Рон-Пуленк Роре С.А. (FR)
Publication of RU94041682A publication Critical patent/RU94041682A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00Electrolytic production of organic compounds
    • C25B3/20Processes
    • C25B3/25Reduction
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D305/00Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms
    • C07D305/14Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms condensed with carbocyclic rings or ring systems
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B11/00Electrodes; Manufacture thereof not otherwise provided for
    • C25B11/04Electrodes; Manufacture thereof not otherwise provided for characterised by the material
    • C25B11/042Electrodes formed of a single material
    • C25B11/043Carbon, e.g. diamond or graphene
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25BELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B11/00Electrodes; Manufacture thereof not otherwise provided for
    • C25B11/04Electrodes; Manufacture thereof not otherwise provided for characterised by the material
    • C25B11/042Electrodes formed of a single material
    • C25B11/046Alloys

Abstract

FIELD: organic chemistry. SUBSTANCE: electrochemical method of synthesis of taxane derivatives of the general formula(I) from the compound of the general formula(II). In general formula (I)Ar means aryl radical, Rmeans benzol radical or radical R-O-CO- in which Rmeans radical of alkyl, alkenyl, alkinyl, cycloalkyl, cycloalkenyl, bicycloalkenyl, phenyl or heterocyclyl and R means hydrogen atom or acetyl radical. In general formula (II)Ar and R were defined as in general formula (I); R′ means acetyl radical or 2,2,2-trichloroethoxycarbonyl and Gmeans radical 2,2,2-trichloroethoxycarbonyl and Gmeans hydrogen atom. Compounds of the general formula (I)show strong antitumor properties. EFFECT: improved method of synthesis.

Claims (1)

Объектом изобретения является электрохимический способ получения производных таксана общей формулы I, указанной в описании, исходя из продукта общей формулы II, указанной в описании. Продукты общей формулы I имеют замечательные противоопухолевые свойства.The object of the invention is an electrochemical method for producing taxane derivatives of the general formula I specified in the description, based on the product of the general formula II specified in the description. The products of general formula I have remarkable antitumor properties.
RU94041682/04A 1992-03-13 1994-09-12 Method of synthesis of taxane derivatives RU94041682A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9203000A FR2688518B1 (en) 1992-03-13 1992-03-13 PROCESS FOR THE PREPARATION OF TAXANE DERIVATIVES.
FR9203000 1992-03-13

Publications (1)

Publication Number Publication Date
RU94041682A true RU94041682A (en) 1996-07-20

Family

ID=9427641

Family Applications (1)

Application Number Title Priority Date Filing Date
RU94041682/04A RU94041682A (en) 1992-03-13 1994-09-12 Method of synthesis of taxane derivatives

Country Status (21)

Country Link
EP (1) EP0630428B1 (en)
JP (1) JPH07504461A (en)
KR (1) KR950700439A (en)
AT (1) ATE130053T1 (en)
AU (1) AU3756393A (en)
CA (1) CA2117552A1 (en)
CZ (1) CZ218694A3 (en)
DE (1) DE69300766T2 (en)
DK (1) DK0630428T3 (en)
ES (1) ES2079982T3 (en)
FI (1) FI944190A (en)
FR (1) FR2688518B1 (en)
GR (1) GR3018036T3 (en)
HU (1) HUT68282A (en)
MX (1) MX9301345A (en)
NO (1) NO943371L (en)
RU (1) RU94041682A (en)
SK (1) SK108494A3 (en)
TW (1) TW235961B (en)
WO (1) WO1993018210A1 (en)
ZA (1) ZA931800B (en)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6794523B2 (en) 1991-09-23 2004-09-21 Florida State University Taxanes having t-butoxycarbonyl substituted side-chains and pharmaceutical compositions containing them
PT1227093E (en) * 1993-03-22 2005-09-30 Univ Florida State BETA-CACTAMAS UTEIS FOR THE PREPARATION OF TAXANS HAVING REPLACED LATERAL CHAIN WITH FURY OR TIENYL
US5760251A (en) * 1995-08-11 1998-06-02 Sepracor, Inc. Taxol process and compounds
US6103698A (en) 1997-03-13 2000-08-15 Basf Aktiengesellschaft Dolastatin-15 derivatives in combination with taxanes
DK2264172T3 (en) 2002-04-05 2017-11-27 Roche Innovation Ct Copenhagen As Oligomeric Compounds for Modulating HIF-1α Expression
US7713738B2 (en) 2003-02-10 2010-05-11 Enzon Pharmaceuticals, Inc. Oligomeric compounds for the modulation of survivin expression
KR20070006709A (en) 2003-12-23 2007-01-11 산타리스 팔마 에이/에스 Oligomeric compounds for the modulation of bcl-2
US9447138B2 (en) 2004-11-09 2016-09-20 Roche Innovation Center Copenhagen A/S Potent LNA oligonucleotides for the inhibition of HIF-1a expression
BRPI0517613A (en) 2004-11-09 2008-10-14 Santaris Pharma As oligonucleotides lna and cancer treatment
EP1833840B9 (en) 2004-11-09 2010-11-10 Santaris Pharma A/S Potent lna oligonucleotides for the inhibition of hif-1a

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60187689A (en) * 1984-03-06 1985-09-25 Otsuka Chem Co Ltd Nanufacture of 3-exo-methylenecepham derivative
FR2601675B1 (en) * 1986-07-17 1988-09-23 Rhone Poulenc Sante TAXOL DERIVATIVES, THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
FR2629818B1 (en) * 1988-04-06 1990-11-16 Centre Nat Rech Scient PROCESS FOR THE PREPARATION OF TAXOL
FR2664894A1 (en) * 1990-07-19 1992-01-24 Rhone Poulenc Sante NOVEL STREPTOGRAMIN DERIVATIVES AND THEIR PREPARATION.

Also Published As

Publication number Publication date
GR3018036T3 (en) 1996-02-29
ATE130053T1 (en) 1995-11-15
CA2117552A1 (en) 1993-09-16
KR950700439A (en) 1995-01-16
HUT68282A (en) 1995-04-03
ZA931800B (en) 1993-09-30
TW235961B (en) 1994-12-11
DE69300766D1 (en) 1995-12-14
EP0630428B1 (en) 1995-11-08
JPH07504461A (en) 1995-05-18
EP0630428A1 (en) 1994-12-28
FI944190A0 (en) 1994-09-12
CZ218694A3 (en) 1995-02-15
DE69300766T2 (en) 1996-04-18
FR2688518B1 (en) 1994-05-06
DK0630428T3 (en) 1995-12-27
SK108494A3 (en) 1995-02-08
FR2688518A1 (en) 1993-09-17
HU9402614D0 (en) 1994-11-28
AU3756393A (en) 1993-10-05
FI944190A (en) 1994-09-12
WO1993018210A1 (en) 1993-09-16
NO943371D0 (en) 1994-09-12
NO943371L (en) 1994-09-12
MX9301345A (en) 1993-09-01
ES2079982T3 (en) 1996-01-16

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